5 results
·
52ms
·
Sources: EU EUDAMED, US FDA
Filters
FDA Recall
×
xTAG Gastrointestinal Pathogen Panel intended for the simultaneous qualitative detection and identification of multiple viral, bacterial and parasitic nucleic acids in human stool specimens or human stool (GPP) Kit, IVD, REF I032C0316.
FDA Recall
Open, Classified
·Luminex Molecular Diagnostics·Product code PCH·February 22, 2019
xTAG Respiratory Viral Panel (RVP): Box Label: xTAG RVP (Respiratory Viral Panel). Catalogue Number:I019C0111 in vitro diagnostic test
FDA Recall
Open, Classified
·Luminex Molecular Diagnostics·Product code OCC·July 16, 2019
xTAG CYP2D6 Kit v3 IVD For use with Luminex 100/200 Instrument Luminex Molecular Diagnostics, Inc. 439 University Ave. Toronto, Ontario Canada Catalog # I030B0373 The xTAG CYP2D6 Kit v3 is a device used to simultaneously detect and identify a panel of nucleotide variants found within the highly polymorphic CYP2D6 gene located on chromosome 22 from genomic DNA extracted from EDTA and citrate anticoagulated whole blood samples.
FDA Recall
Terminated
·Luminex Corporation·Product code NTI·May 24, 2011
NxTAG Respiratory Pathogen Panel +SARS-CoV-2, REF: I056C0468
FDA Recall
Open, Classified
·Luminex Molecular Diagnostics Inc·Product code QLT·September 5, 2024
NxTAG Respiratory Pathogen Panel, REF: I051C0447
FDA Recall
Open, Classified
·Luminex Molecular Diagnostics Inc·Product code OCC·September 5, 2024